HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
Acetone → 9H-xanthene-9-carboxylic acid (5-ethyl-[1,3,4]oxadiazol-2-yl)amide
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | Acetone | HCID 180 | — |
| Edukt | 5-Ethyl-1,3,4-oxadiazol-2-amine | HCID 343487 | — |
| Edukt | (3,5-dimethylpyrazol-1-yl)-(9H-xanthen-9-yl)methanone | HCID 4521579 | — |
| Lösungsmittel | Dimethylformamide | HCID 6228 | — |
| Produkt | 9H-xanthene-9-carboxylic acid (5-ethyl-[1,3,4]oxadiazol-2-yl)amide | HCID 53922562 | 41,7% |
Reaktionsschritte
500.5 mg (1.64 mmol) (3.5-dimethylpyrazol-1-yl)-(9H-xanthen-9-yl)-methanone and 186.8 mg (1.64 mmol) 5-ethyl-[1,3,4]oxadiazol-2-ylamine were suspended in 1.5 ml DMF and stirred for 6 h at 130°. The reaction mixture was allowed to cool to room temperature and 5 ml of acetone were added. After stirring for 5 min, the product was filtered, washed with acetone and dried in vaccuo to yield 219.5 mg of 9H-xanthene-9-carboxylic acid (5-ethyl-[1,3,4]oxadiazol-2-yl)-amide as a white solid, m.p. 256-257° C. and MS: m/e=321.2 (M+) 48b) The 5-ethyl-[1,3,4]oxadiazol-2-ylamine used in the above reaction was obtained as follows:
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US06462198B1 |
| Quelldatensatz | uspto-grants-2002_10 |
| ORD ID | ord-d3f66ded2c674e3ea58617552df29109 |
| Quellennotiz | uspto-grants-2002_10 |